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Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment

The aim of the study was to evaluate the association between genetic polymorphisms of CYP2D6 and outcomes in breast cancer patients with tamoxifen treatment. We evaluated the CYP2D6 genetic polymorphisms in 766 breast cancer patients. Among them, 110 patients whose samples were prospectively collect...

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Autores principales: Park, Hyung Seok, Choi, Ji-Yeob, Lee, Mi-Jeong, Park, Seho, Yeo, Chang-Woo, Lee, Sang Seop, Shin, Jae-Gook, Park, Byeong-Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154335/
https://www.ncbi.nlm.nih.gov/pubmed/21860550
http://dx.doi.org/10.3346/jkms.2011.26.8.1007
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author Park, Hyung Seok
Choi, Ji-Yeob
Lee, Mi-Jeong
Park, Seho
Yeo, Chang-Woo
Lee, Sang Seop
Shin, Jae-Gook
Park, Byeong-Woo
author_facet Park, Hyung Seok
Choi, Ji-Yeob
Lee, Mi-Jeong
Park, Seho
Yeo, Chang-Woo
Lee, Sang Seop
Shin, Jae-Gook
Park, Byeong-Woo
author_sort Park, Hyung Seok
collection PubMed
description The aim of the study was to evaluate the association between genetic polymorphisms of CYP2D6 and outcomes in breast cancer patients with tamoxifen treatment. We evaluated the CYP2D6 genetic polymorphisms in 766 breast cancer patients. Among them, 110 patients whose samples were prospectively collected before surgery and treated with tamoxifen were included to evaluate the association between CYP2D6 and outcomes. The genotypes of CYP2D6 were categorized as extensive metabolizer (EM), intermediate metabolizer (IM), and poor metabolizer (PM) according to the activity score. The clinicopathologic features of 110 patients were not significantly different among the three groups except for the T-stage and nodal status. The high T-stage and axillary metastasis were more frequent in the PM group. While recurrence-free and overall survival in the PM group was poorer than the other groups, there was no significant difference between the EM and the IM group. The difference between the PM and the other groups on univariate analysis disappeared on multivariate analysis. These conflicting results suggest that the clinical value of CYP2D6 polymorphisms is still unclear and more large-sized and comprehensively designed trials are necessary.
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spelling pubmed-31543352011-08-22 Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment Park, Hyung Seok Choi, Ji-Yeob Lee, Mi-Jeong Park, Seho Yeo, Chang-Woo Lee, Sang Seop Shin, Jae-Gook Park, Byeong-Woo J Korean Med Sci Original Article The aim of the study was to evaluate the association between genetic polymorphisms of CYP2D6 and outcomes in breast cancer patients with tamoxifen treatment. We evaluated the CYP2D6 genetic polymorphisms in 766 breast cancer patients. Among them, 110 patients whose samples were prospectively collected before surgery and treated with tamoxifen were included to evaluate the association between CYP2D6 and outcomes. The genotypes of CYP2D6 were categorized as extensive metabolizer (EM), intermediate metabolizer (IM), and poor metabolizer (PM) according to the activity score. The clinicopathologic features of 110 patients were not significantly different among the three groups except for the T-stage and nodal status. The high T-stage and axillary metastasis were more frequent in the PM group. While recurrence-free and overall survival in the PM group was poorer than the other groups, there was no significant difference between the EM and the IM group. The difference between the PM and the other groups on univariate analysis disappeared on multivariate analysis. These conflicting results suggest that the clinical value of CYP2D6 polymorphisms is still unclear and more large-sized and comprehensively designed trials are necessary. The Korean Academy of Medical Sciences 2011-08 2011-07-27 /pmc/articles/PMC3154335/ /pubmed/21860550 http://dx.doi.org/10.3346/jkms.2011.26.8.1007 Text en © 2011 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Hyung Seok
Choi, Ji-Yeob
Lee, Mi-Jeong
Park, Seho
Yeo, Chang-Woo
Lee, Sang Seop
Shin, Jae-Gook
Park, Byeong-Woo
Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment
title Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment
title_full Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment
title_fullStr Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment
title_full_unstemmed Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment
title_short Association between Genetic Polymorphisms of CYP2D6 and Outcomes in Breast Cancer Patients with Tamoxifen Treatment
title_sort association between genetic polymorphisms of cyp2d6 and outcomes in breast cancer patients with tamoxifen treatment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154335/
https://www.ncbi.nlm.nih.gov/pubmed/21860550
http://dx.doi.org/10.3346/jkms.2011.26.8.1007
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